MicroRNA-34c-5p is related to recurrence in laryngeal squamous cell carcinoma

Altered microRNA expression has been found in many cancer types, including laryngeal squamous cell carcinoma (LSCC). We investigated the association of LSCC-related miR-34c-5p with disease-free survival and overall survival. Retrospective cohort study. Expression levels of miR-34c-5p were detected i...

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Published inThe Laryngoscope Vol. 125; no. 9; p. E306
Main Authors Re, Massimo, Çeka, Artan, Rubini, Corrado, Ferrante, Luigi, Zizzi, Antonio, Gioacchini, Federico M, Tulli, Michele, Spazzafumo, Liana, Sellari-Franceschini, Stefano, Procopio, Antonio D, Olivieri, Fabiola
Format Journal Article
LanguageEnglish
Published United States 01.09.2015
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ISSN1531-4995
DOI10.1002/lary.25475

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Abstract Altered microRNA expression has been found in many cancer types, including laryngeal squamous cell carcinoma (LSCC). We investigated the association of LSCC-related miR-34c-5p with disease-free survival and overall survival. Retrospective cohort study. Expression levels of miR-34c-5p were detected in 90 LSCC formalin-fixed paraffin-embedded tissues by reverse-transcription quantitative polymerase chain reaction. Overall survival and disease-free survival were evaluated using the Kaplan-Meier method, and multivariate analysis was performed using Cox proportional hazard analysis. A downregulation of miR-34c-5p expression significantly correlated with worse disease-free and overall survival. In the multivariate analysis, low miR-34c-5p expression was associated with an increased risk of recurrence. A downregulation of miR-34c-5p in LSCC is independently associated with unfavorable disease-free survival, suggesting that miR-34c-5p might be a promising marker for evaluating the risk of recurrences. NA.
AbstractList Altered microRNA expression has been found in many cancer types, including laryngeal squamous cell carcinoma (LSCC). We investigated the association of LSCC-related miR-34c-5p with disease-free survival and overall survival. Retrospective cohort study. Expression levels of miR-34c-5p were detected in 90 LSCC formalin-fixed paraffin-embedded tissues by reverse-transcription quantitative polymerase chain reaction. Overall survival and disease-free survival were evaluated using the Kaplan-Meier method, and multivariate analysis was performed using Cox proportional hazard analysis. A downregulation of miR-34c-5p expression significantly correlated with worse disease-free and overall survival. In the multivariate analysis, low miR-34c-5p expression was associated with an increased risk of recurrence. A downregulation of miR-34c-5p in LSCC is independently associated with unfavorable disease-free survival, suggesting that miR-34c-5p might be a promising marker for evaluating the risk of recurrences. NA.
Author Procopio, Antonio D
Re, Massimo
Olivieri, Fabiola
Sellari-Franceschini, Stefano
Gioacchini, Federico M
Ferrante, Luigi
Spazzafumo, Liana
Rubini, Corrado
Çeka, Artan
Zizzi, Antonio
Tulli, Michele
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Issue 9
Keywords recurrence
microRNA
miR-34c-5p
Laryngeal squamous cell carcinoma
prognosis
biomarkers
Language English
License 2015 The American Laryngological, Rhinological and Otological Society, Inc.
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Snippet Altered microRNA expression has been found in many cancer types, including laryngeal squamous cell carcinoma (LSCC). We investigated the association of...
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StartPage E306
SubjectTerms Aged
Aged, 80 and over
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - mortality
Carcinoma, Squamous Cell - pathology
Female
Follow-Up Studies
Gene Expression Regulation, Neoplastic
Humans
Italy - epidemiology
Laryngeal Neoplasms - genetics
Laryngeal Neoplasms - mortality
Laryngeal Neoplasms - pathology
Male
MicroRNAs - genetics
Middle Aged
Neoplasm Recurrence, Local - genetics
Neoplasm Recurrence, Local - mortality
Neoplasm Recurrence, Local - pathology
Neoplasm Staging
Prognosis
Real-Time Polymerase Chain Reaction
Retrospective Studies
RNA, Neoplasm - genetics
Title MicroRNA-34c-5p is related to recurrence in laryngeal squamous cell carcinoma
URI https://www.ncbi.nlm.nih.gov/pubmed/26153151
Volume 125
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